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Senior Clinical Research Coordinator
1 month ago
Vitalief is a pioneering healthcare consulting company dedicated to empowering research and transforming clinical trials. We're seeking a highly skilled and enthusiastic Senior Clinical Research Coordinator to join our exceptional team and contribute to our mission of advancing scientific discoveries that can change patients' lives for the better.
Why Choose Vitalief?- We prioritize personal and professional growth for all our employees, fostering a culture of innovation and collaboration.
- Our employees enjoy a competitive salary range, 20 PTO days, 9 paid holidays, and comprehensive benefits, including company-paid life insurance and short/long-term disability coverage.
- We offer a robust 401K retirement program and a range of healthcare plans to choose from.
- Develop and implement clinical research trials, ensuring compliance with Good Clinical Practices, HIPAA, and regulatory requirements.
- Collaborate with internal and external stakeholders, including patients, principal investigators, and sponsors.
- Oversee research IRB projects, ensuring accurate execution and adherence to hospital IRB protocol, policies, and procedures.
- Provide guidance to research support staff and work autonomously with limited oversight on projects.
- Bachelor's degree in Business Administration, Healthcare Administration, or a related field.
- Minimum 3-4 years of experience in clinical research trials coordination, with a strong understanding of coordination requirements and Good Clinical Practices.
- Excellent communication, interpersonal, and time management skills, with the ability to multitask and work independently.
Standing, sitting, walking, visual perception, talking, and hearing. Lifting up to 20lbs.
Vitalief partners with clients such as major medical centers and academic institutions, requiring all on-site resources to be inoculated annually for Influenza and successfully pass a Mantoux Tuberculin Skin Test (TST) for Mycobacterium Tuberculosis.